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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608596Generated: October 26, 2026

Triethylamine → 5-[2-(Ethylsulfonylamino)ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1608596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridineHCID 15229369—
SolventDichloromethaneHCID 6344—
Product5-[2-(Ethylsulfonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 1522936478.2%

Reaction Steps

To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (1.93 g, 10 mmoles) and triethylamine (1.53 ml, 11 mmoles) in methylene chloride (100 ml) was added ethanesulfonyl chloride (0.95 ml, 10 mmoles) at room temperature with stirring and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and water and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:5) to obtain 2.23 g of the desired product (78.2%, colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-78fececa60d143e3b0db984b9b53dc46
Source noteuspto-grants-1995_03